215029-48-4

Basic information

• Product Name: H₂N-Ala-Val-OBn
• Synonyms: H₂N-Ala-Val-OBn
• CAS NO: 215029-48-4
• Molecular Weight: 278.351
• Mol File: 215029-48-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: H₂N-Ala-Val-OBn(CAS DataBase Reference)
• NIST Chemistry Reference: H₂N-Ala-Val-OBn(215029-48-4)
• EPA Substance Registry System: H₂N-Ala-Val-OBn(215029-48-4)

Safety Data

• Hazardous Substances Data: 215029-48-4(Hazardous Substances Data)

Upstream product

• 116912-11-9 N-(Phenylacetyl)-L-alanyl-L-valin-benzylester 
• 21760-98-5 L-valine benzyl ester 
• 116798-35-7 Boc-L-Ala-L-Val-OBzl 

Downstream Products

• 1087223-98-0 C₃₃H₄₆N₆O₆ 
• 1242760-39-9 Boc-Val-Ala-Val-OCH₂Ph 
• 532926-64-0 Boc-A-A-V-OCH₂Ph 

Relevant articles and documents

Development of supramolecular organo-gel based on tripeptide skeletons

Boc-Ser-Val-Gly-OCH2Ph (31) showed high gelation abilities in the aromatic solvents, particularly in toluene. The minimum gelation concentration of 31 in toluene was 10 mg/ml, suggesting that 2500 molecules of toluene were immobilized by each m

THE USE OF PENICILLIN ACYLASE FOR SELECTIVE N-TERMINAL DEPROTECTION IN PEPTIDE SYNTHESIS

Penicillin acylase from E. coli (EC 3.5.1.11) accepts a broad range of N-phenylacetyl-dipeptide esters as substrates.The enzyme hydrolyses the N-terminal protecting group selectively at room temp. and pH=8.1 without affecting the peptide- or the ester-bonds.Alternatively methyl-, benzyl-, tert-butyl and allyl esters can be cleaved chemically leaving the phenylacetamido moiety intact.